ClinVar Miner

Submissions for variant NM_000169.3(GLA):c.201G>A (p.Lys67=)

dbSNP: rs2147480934
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002141197 SCV002461051 likely benign Fabry disease 2022-02-05 criteria provided, single submitter clinical testing

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